Transcriptional co-activator activity of SYT is negatively regulated by BRM and Brg1

被引:20
|
作者
Ishida, M
Tanaka, S
Ohki, M
Ohta, T
机构
[1] Natl Canc Ctr, Res Inst, Ctr Med Genom, Chuo Ku, Tokyo 1040045, Japan
[2] Hokkaido Univ, Sch Med, Lab Mol & Cellular Pathol, Kita Ku, Sapporo, Hokkaido 0608638, Japan
关键词
D O I
10.1111/j.1356-9597.2004.00737.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The t(X;18)(p11.2;q11.2) translocation found in synovial sarcomas results in the fusion of the SYT gene on chromosome 18 to the SSX gene on chromosome X. Although the SYT-SSX fusion proteins may trigger synovial sarcoma development, the biological functions of SYT, SSX and SYT-SSX genes are unclear. Transfections of Gal4 DNA binding domain fusion protein constructs demonstrate that SYT protein acts as a transcriptional co-activator at the C-terminal domain and that the activity is repressed through the N-terminus. The N-terminal 70 amino acids of SYT bind not only to BRM, but also to Brg1, both of which are subunits of SWI/SNF chromatin remodelling complexes. Here, we have investigated the functions of BRM and Brg1 on the repression of SYT activity. The negative regulation of SYT transcriptional co-activator activity is dependent on the ATP-hydrolysis of BRM and Brg1 in the protein complexes. This indicates that the SWI/SNF protein complexes regulate SYT activity using the chromatin remodelling activity.
引用
收藏
页码:419 / 428
页数:10
相关论文
共 50 条
  • [31] A function of CBP as a transcriptional co-activator during Dpp signalling
    Waltzer, L
    Bienz, M
    EMBO JOURNAL, 1999, 18 (06): : 1630 - 1641
  • [32] Characterization of Phosphopeptide Positional Isomers on the Transcriptional Co-activator TAZ
    Roberto, Justin
    Sykes, Catherine E.
    Vacratsis, Panayiotis O.
    BIOCHEMISTRY, 2020, 59 (43) : 4148 - 4154
  • [33] Life and death of transcriptional co-activator p300
    Chen, Jihong
    Li, Qiao
    EPIGENETICS, 2011, 6 (08) : 957 - 961
  • [34] Nuclear IGF1R is a transcriptional co-activator of LEF1/TCF
    Warsito, Dudi
    Sjostrom, Sylvia
    Andersson, Sandra
    Larsson, Olle
    Sehat, Bita
    EMBO REPORTS, 2012, 13 (03) : 244 - 250
  • [35] Targeting Transcriptional Co-Activator PGC-1a for the Treatment of Sickle Cell Disease
    Habara, Alawi
    Le, Cuong
    Chui, David H. K.
    Steinberg, Martin H.
    Cui, Shuaiying
    BLOOD, 2019, 134
  • [36] INVESTIGATING THE ROLE OF THE TRANSCRIPTIONAL CO-ACTIVATOR TAZ IN ALVEOLAR RHABDOMYOSARCOMA
    Deel, Michael
    Slemmons, Katrina
    Bentley, Rex
    Linardie, Corinne
    PEDIATRIC BLOOD & CANCER, 2016, 63 : S63 - S64
  • [37] E2F6 Associates with BRG1 in Transcriptional Regulation
    Leung, Janet Y.
    Nevins, Joseph R.
    PLOS ONE, 2012, 7 (10):
  • [38] Co-activator SRC-1 is dispensable for transcriptional control by STAT3
    Cvijic, Helena
    Bauer, Kay
    Loeffler, Dennis
    Pfeifer, Gabriele
    Blumert, Conny
    Kretzschmar, Antje K.
    Henze, Christian
    Brocke-Heidrich, Katja
    Horn, Friedernann
    BIOCHEMICAL JOURNAL, 2009, 420 : 123 - 132
  • [39] Alternative isoforms of BmYki have different transcriptional co-activator activity in the silkworm, Bombyx mori
    Liang, Zi
    Lu, Yahong
    Jiang, Mengsheng
    Qian, Ying
    Zhu, Liyuan
    Kuang, Sulan
    Chen, Fei
    Feng, Yongjie
    Hu, Xiaolong
    Cao, Guangli
    Xue, Renyu
    Gong, Chengliang
    INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2019, 116
  • [40] An insight into structural plasticity and conformational transitions of transcriptional co-activator Sus1
    Bharati, Akhilendra Pratap
    Kashif, Mohd
    Chaturvedi, Sumit Kumar
    Khan, Rizwan Hasan
    Ahmad, Abrar
    PLOS ONE, 2020, 15 (03):